Canonical Allele Identifier: CA2213436389

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641081T= , CM000678.2:g.23641081T=	GRCh38
NC_000016.9:g.23652402T= , CM000678.1:g.23652402T=	GRCh37
NC_000016.8:g.23559903T=	NCBI36
NG_007406.1:g.5277A= , LRG_308:g.5277A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-776A=	ENSP00000460666.3:n.-776A=
ENST00000565038.2:c.48+29A=	ENSP00000459882.2:n.48+29A=
ENST00000566069.6:c.48+29A=	ENSP00000459237.2:n.48+29A=
ENST00000697377.2:c.-192+29A=	ENSP00000513286.2:n.-192+29A=
ENST00000697379.2:c.-98+29A=	ENSP00000513287.2:n.-98+29A=
ENST00000561514.2:c.-1667A=	ENSP00000460666.2:n.-1667A=
ENST00000697374.1:c.-1258A=	ENSP00000513284.1:n.-1258A=
ENST00000697376.1:c.-1008+29A=	ENSP00000513285.1:n.-1008+29A=
ENST00000697377.1:c.-1083+29A=	ENSP00000513286.1:n.-1083+29A=
ENST00000697379.1:c.-989+29A=	ENSP00000513287.1:n.-989+29A=
ENST00000697382.1:c.-1718A=	ENSP00000513288.1:n.-1718A=
ENST00000697383.1:c.48+29A=	ENSP00000513289.1:n.48+29A=
ENST00000697384.1:n.202+29A=
ENST00000261584.9:c.48+29A= MANE Select	ENSP00000261584.4:n.48+29A=
ENST00000261584.8:c.48+29A=	ENSP00000261584.4:n.48+29A=
ENST00000567003.1:n.192+29A=
ENST00000568219.5:c.-838+46A=	ENSP00000454703.2:n.-838+46A=
NM_024675.3:c.48+29A= , LRG_308t1:c.48+29A=	NP_078951.2:n.48+29A=
XM_011545946.1:c.-776A=	XP_011544248.1:n.-776A=
XM_011545947.1:c.-776A=	XP_011544249.1:n.-776A=
XM_011545948.1:c.-972+29A=	XP_011544250.1:n.-972+29A=
XR_950851.1:n.15A=
XM_011545946.2:c.-776A=	XP_011544248.1:n.-776A=
XM_011545947.2:c.-776A=	XP_011544249.1:n.-776A=
XM_011545948.2:c.-972+29A=	XP_011544250.1:n.-972+29A=
XM_017023671.1:c.-776A=	XP_016879160.1:n.-776A=
XM_017023672.2:c.48+29A=	XP_016879161.1:n.48+29A=
XM_017023673.2:c.48+29A=	XP_016879162.1:n.48+29A=
NM_024675.4:c.48+29A= MANE Select	NP_078951.2:n.48+29A=